Literature DB >> 26077818

Single-Cell Whole-Genome Amplification and Sequencing: Methodology and Applications.

Lei Huang1, Fei Ma, Alec Chapman, Sijia Lu, Xiaoliang Sunney Xie.   

Abstract

We present a survey of single-cell whole-genome amplification (WGA) methods, including degenerate oligonucleotide-primed polymerase chain reaction (DOP-PCR), multiple displacement amplification (MDA), and multiple annealing and looping-based amplification cycles (MALBAC). The key parameters to characterize the performance of these methods are defined, including genome coverage, uniformity, reproducibility, unmappable rates, chimera rates, allele dropout rates, false positive rates for calling single-nucleotide variations, and ability to call copy-number variations. Using these parameters, we compare five commercial WGA kits by performing deep sequencing of multiple single cells. We also discuss several major applications of single-cell genomics, including studies of whole-genome de novo mutation rates, the early evolution of cancer genomes, circulating tumor cells (CTCs), meiotic recombination of germ cells, preimplantation genetic diagnosis (PGD), and preimplantation genomic screening (PGS) for in vitro-fertilized embryos.

Entities:  

Keywords:  CTC; DOP-PCR; MALBAC; MDA; PGD; PGS; WGA; cancer genomics; in vitro fertilization; single-cell genomics

Mesh:

Year:  2015        PMID: 26077818     DOI: 10.1146/annurev-genom-090413-025352

Source DB:  PubMed          Journal:  Annu Rev Genomics Hum Genet        ISSN: 1527-8204            Impact factor:   8.929


  127 in total

Review 1.  Single-cell epigenomics: techniques and emerging applications.

Authors:  Omer Schwartzman; Amos Tanay
Journal:  Nat Rev Genet       Date:  2015-10-13       Impact factor: 53.242

Review 2.  Single-cell genome sequencing: current state of the science.

Authors:  Charles Gawad; Winston Koh; Stephen R Quake
Journal:  Nat Rev Genet       Date:  2016-01-25       Impact factor: 53.242

Review 3.  Detecting Somatic Mutations in Normal Cells.

Authors:  Yanmei Dou; Heather D Gold; Lovelace J Luquette; Peter J Park
Journal:  Trends Genet       Date:  2018-05-03       Impact factor: 11.639

4.  Single-cell whole-genome analyses by Linear Amplification via Transposon Insertion (LIANTI).

Authors:  Chongyi Chen; Dong Xing; Longzhi Tan; Heng Li; Guangyu Zhou; Lei Huang; X Sunney Xie
Journal:  Science       Date:  2017-04-14       Impact factor: 47.728

5.  Noninvasive preimplantation genetic testing for aneuploidy in spent medium may be more reliable than trophectoderm biopsy.

Authors:  Lei Huang; Berhan Bogale; Yaqiong Tang; Sijia Lu; Xiaoliang Sunney Xie; Catherine Racowsky
Journal:  Proc Natl Acad Sci U S A       Date:  2019-06-24       Impact factor: 11.205

6.  DNA copy number profiling using single-cell sequencing.

Authors:  Xuefeng Wang; Hao Chen; Nancy R Zhang
Journal:  Brief Bioinform       Date:  2018-09-28       Impact factor: 11.622

7.  Genotyping single-sperm cells by universal MARSALA enables the acquisition of linkage information for combined pre-implantation genetic diagnosis and genome screening.

Authors:  Haitao Wu; Xiaoting Shen; Lei Huang; Yanhong Zeng; Yumei Gao; Lin Shao; Baomin Lu; Yiping Zhong; Benyu Miao; Yanwen Xu; Yali Wang; Yubin Li; Luoxing Xiong; Sijia Lu; X Sunney Xie; Canquan Zhou
Journal:  J Assist Reprod Genet       Date:  2018-05-22       Impact factor: 3.412

Review 8.  Tumour heterogeneity and metastasis at single-cell resolution.

Authors:  Devon A Lawson; Kai Kessenbrock; Ryan T Davis; Nicholas Pervolarakis; Zena Werb
Journal:  Nat Cell Biol       Date:  2018-11-26       Impact factor: 28.824

9.  Comparative genomics of CXCR4MUT and CXCR4WT single cells in Waldenström's macroglobulinemia.

Authors:  Cristina Jiménez; Lian Xu; Nickolas Tsakmaklis; Maria G Demos; Amanda Kofides; Gloria G Chan; Maria Luisa Guerrera; Jiaji G Chen; Xia Liu; Manit Munshi; Christopher J Patterson; Guang Yang; Jorge J Castillo; Steven P Treon; Zachary R Hunter
Journal:  Blood Adv       Date:  2020-09-22

10.  Evolution and heterogeneity of non-hereditary colorectal cancer revealed by single-cell exome sequencing.

Authors:  H Wu; X-Y Zhang; Z Hu; Q Hou; H Zhang; Y Li; S Li; J Yue; Z Jiang; S M Weissman; X Pan; B-G Ju; S Wu
Journal:  Oncogene       Date:  2016-12-12       Impact factor: 9.867

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